Efficacy and Safety of Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Across Various Age Groups: A Systematic Review
Abstract
1. Introduction
2. Materials and Methods
2.1. Search Strategy
2.2. Study Selection
2.2.1. Inclusion Criteria
2.2.2. Exclusion Criteria
2.2.3. Screening and Data Extraction
2.2.4. Quality Assessment and Bias Evaluation
2.3. Data Synthesis and Statistical Analysis
Age Grouping and Subgroup Analysis
2.4. OSA Severity Classification
3. Result
3.1. Study Selection and Characteristics
3.2. Age-Specific Response to Adenotonsillectomy
3.2.1. Reduction in Apnea-Hypopnea Index (AHI)
3.2.2. Oxygen Desaturation Index (ODI) and Sleep Quality
3.2.3. Neurocognitive and Behavioral Improvements
3.2.4. Surgical Safety and Complications
3.3. Long-Term Follow-Up Outcomes Post-Adenotonsillectomy
4. Discussion
4.1. Strengths
4.2. Limitations
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Conflicts of Interest
Abbreviations
AT | Adenotonsillectomy |
OSA | Obstructive sleep apnea |
PSG | Polysomnography |
PRISMA | Preferred Reporting Items for Systematic Reviews and Meta-Analyses |
MeSH | Medical Subject Headings |
RCTs | Randomized controlled trials |
BMI | Body mass index |
NOS | Newcastle−Ottawa Scale |
GRADE | Grading of Recommendations, Assessment, Development, and Evaluations |
CIs | Confidence intervals |
AHI | Apnea-hypopnea index |
SDB | Sleep-disordered breathing |
PG | Pulmonary gas |
LTRAs | Leukotriene receptor antagonists |
OAI | Obstructive apnea index |
RDI | Respiratory disturbance index |
VMI | Visual-motor integration |
BP | Blood pressure |
BNP | B-type natriuretic peptide |
A/N | Adenoidal/Nasopharyngeal |
PICU | Pediatric intensive care unit |
IQ | Intelligence quotient |
ENT | Ear, Nose, and Throat |
ODI | Oxygen desaturation index |
PAP | Positive airway pressure |
Appendix A
Section and Topic | Item | Checklist Item | Location Where Item Is Reported |
---|---|---|---|
TITLE | |||
Title | 1 | Identify the report as a systematic review. | Page 1; lines 2 to 4 |
ABSTRACT | |||
Abstract | 2 | See the PRISMA 2020 for Abstracts checklist. | Page 1; lines 28 to 43 |
INTRODUCTION | |||
Rationale | 3 | Describe the rationale for the review in the context of existing knowledge. | Page 2; lines 48 to 61 |
Objectives | 4 | Provide an explicit statement of the objective(s) or question(s) the review addresses. | Page 2; lines 78 to 90 |
METHODS | |||
Eligibility criteria | 5 | Specify the inclusion and exclusion criteria for the review and how studies were grouped for the syntheses. | Page 3; lines 104 to 121 |
Information sources | 6 | Specify all databases, registers, websites, organizations, reference lists and other sources searched or consulted to identify studies. Specify the date when each source was last searched or consulted. | Pages 2 and 3; lines 93 to 103 |
Search strategy | 7 | Present the full search strategies for all databases, registers and websites, including any filters and limits used. | Pages 2 and 3; lines 93 to 103 |
Selection process | 8 | Specify the methods used to decide whether a study met the inclusion criteria of the review, including how many reviewers screened each record and each report retrieved, whether they worked independently, and, if applicable, details of automation tools used in the process. | Page 3; lines 122 to 131 |
Data collection process | 9 | Specify the methods used to collect data from reports, including how many reviewers collected data from each report, whether they worked independently, any processes for obtaining or confirming data from study investigators, and, if applicable, details of automation tools used in the process. | Page 3; lines 122 to 131 |
Data items | 10a | List and define all outcomes for which data were sought. Specify whether all results that were compatible with each outcome domain in each study were sought (e.g., for all measures, time points, analyses), and if not, the methods used to decide which results to collect. | ND |
10b | List and define all other variables for which data were sought (e.g., participant and intervention characteristics, funding sources). Describe any assumptions made about any missing or unclear information. | ND | |
Study risk of bias assessment | 11 | Specify the methods used to assess the risk of bias in the included studies, including details of the tool(s) used, how many reviewers assessed each study and whether they worked independently, and if applicable, details of automation tools used in the process. | Page 3; lines 133 to 143 |
Effect measures | 12 | Specify for each outcome the effect measure(s) (e.g., risk ratio, mean difference) used in the synthesis or presentation of results. | ND |
Synthesis methods | 13a | Describe the processes used to decide which studies were eligible for each synthesis (e.g., tabulating the study intervention characteristics and comparing against the planned groups for each synthesis (item #5)). | Page 4; lines 145 to 169 |
13b | Describe any methods required to prepare the data for presentation or synthesis, such as handling missing summary statistics or data conversions. | Page 4; lines 145 to 169 | |
13c | Describe any methods used to tabulate or visually display the results of individual studies and syntheses. | Page 4; lines 145 to 169 | |
13d | Describe any methods used to synthesize results and provide a rationale for the choice(s). If meta-analysis was performed, describe the model(s), method(s) to identify the presence and extent of statistical heterogeneity, and software package(s) used. | Page 4; lines 145 to 169 | |
13e | Describe any methods used to explore possible causes of heterogeneity among study results (e.g., subgroup analysis, meta-regression). | ND | |
13f | Describe any sensitivity analyses conducted to assess the robustness of the synthesized results. | ND | |
Reporting bias assessment | 14 | Describe any methods used to assess the risk of bias due to missing results in a synthesis (arising from reporting biases). | Page 3; lines 133 to 143 |
Certainty assessment | 15 | Describe any methods used to assess certainty (or confidence) in the body of evidence for an outcome. | ND |
RESULTS | |||
Study selection | 16a | Describe the results of the search and selection process, from the number of records identified in the search to the number of studies included in the review, ideally using a flow diagram. | Page 4; lines 171 to 183 |
16b | Cite studies that might appear to meet the inclusion criteria but which were excluded, and explain why they were excluded. | Page 5; lines 184 to 197 | |
Study characteristics | 17 | Cite each included study and present its characteristics. | Page 6 to 8; lines 189 to 202 |
Risk of bias in studies | 18 | Present assessments of risk of bias for each included study. | Pages 20 and 21 |
Results of individual studies | 19 | For all outcomes, present, for each study: (a) summary statistics for each group (where appropriate) and (b) an effect estimate and its precision (e.g., confidence/credible interval), ideally using structured tables or plots. | Page 6 to 8; lines 189 to 202 |
Results of syntheses | 20a | For each synthesis, briefly summarize the characteristics and risk of bias among contributing studies. | Page 6 to 8; lines 189 to 202 |
20b | Present results of all statistical syntheses conducted. If meta-analysis was done, present for each the summary estimate and its precision (e.g., confidence/credible interval) and measures of statistical heterogeneity. If comparing groups, describe the direction of the effect. | ND | |
20c | Present results of all investigations of possible causes of heterogeneity among study results. | ND | |
20d | Present results of all sensitivity analyses conducted to assess the robustness of the synthesized results. | ND | |
Reporting biases | 21 | Present assessments of risk of bias due to missing results (arising from reporting biases) for each synthesis assessed. | ND |
Certainty of evidence | 22 | Present assessments of certainty (or confidence) in the body of evidence for each outcome assessed. | ND |
DISCUSSION | |||
Discussion | 23a | Provide a general interpretation of the results in the context of other evidence. | Page 10; lines 266 to 272 |
23b | Discuss any limitations of the evidence included in the review. | Page 11; lines 305 to 326 | |
23c | Discuss any limitations of the review processes used. | Page 11; lines 305 to 326 | |
23d | Discuss the implications of the results for practice, policy, and future research. | Page 11; lines 321 to 326 | |
OTHER INFORMATION | |||
Registration and protocol | 24a | Provide registration information for the review, including the register name and registration number, or state that the review was not registered. | Page 2; lines 93 to 96 |
24b | Indicate where the review protocol can be accessed or state that a protocol was not prepared. | Page 2; lines 93 to 96 | |
24c | Describe and explain any amendments to information provided at registration or in the protocol. | Pages 17 to 19 | |
Support | 25 | Describe sources of financial or non-financial support for the review and the role of the funders or sponsors in the review. | Page 12; line 350 |
Competing interests | 26 | Declare any competing interests of review authors. | Page 12; line 358 |
Availability of data, code and other materials | 27 | Report which of the following are publicly available and where they can be found: template data collection forms; data extracted from included studies; data used for all analyses; analytic code; any other materials used in the review. | ND |
Appendix B
| |
Pediatric obstructive sleep apnea (OSA) is a childhood disorder in which upper airway dysfunction causes complete or partial airway obstruction during sleep, leading to decreased oxygen saturation or arousal from sleep [1]. Pediatric OSA is a common childhood disease affecting 1–5% of children [2,3]. Untreated children with OSA are reported with not only, sleep problems, but also cognitive/behavioral deficits and a high risk of cardiovascular morbidity [4], presenting a high socioeconomic and humanistic burden for both family and public health [5]. Clinical guidelines recommend (adeno)tonsillectomy (AT) as the first-line treatment [6]. Previous studies have found several contributing factors associated with poor surgical efficacy, including high body mass index (BMI), the severity of OSA and complicated comorbidities [7,8]. However, given the sustained development of children, the potential pathogenic mechanisms underlying OSA and comorbidities are complicated and may differ among age groups. Therefore, the age at surgery may be related to the efficacy of AT. Statistically, the mean age at adenoidectomy was 42.32 months (range, 9–86 months) [9]. However, the available and compelling data are insufficient to prove the impact of age on AT efficacy. Few retrospective, nonrandomized studies have mentioned that older age is a risk factor for residual OSA [10]. Surgical timing was decided based on general experience and clinical practice. Therefore, evidence-based studies on the efficacy of AT in different age groups are anticipated to support surgical strategies and conduct mechanistic studies in the future. | |
| |
This systematic review aims to determine the role of age in AT efficacy, identify the optimal age for AT treatment and examine whether the reported outcomes differ between age groups in children with Polysomnography (PSG)-confirmed uncomplicated OSA. We aimed to provide evidence-based suggestions for precise AT treatment in childhood. | |
| |
| |
| |
Population, or participants and condition of interest | This includes patients of different ages and genders who have been diagnosed with obstructive sleep apnea in various healthcare settings. The condition of interest for this systematic review research is the efficacy and safety of adenotonsillectomy on pediatric obstructive sleep apnea across various age groups. |
Interventions or exposures |
|
Outcomes of interest | Sleep apnea resolution rates, improvement in sleep quality, prevention of sleep apnea recurrence, and overall health outcomes. |
Setting |
|
Inclusion criteria |
|
Exclusion criteria |
|
| |
Electronic databases |
|
Keywords | (Obstructive sleep apnea OR Adenotonsillectomy OR Pediatric OR Age OR Cardiovascular OR Cognitive behavior performance) |
| |
Quality assessment tools or checklists used with references or URLs | Protocol will define the method of literature critique/appraisal use and will use the STROBE tool for relevant content and methodology used in each of the papers to be reviewed. |
Narrative synthesis details what and how synthesis will be done | Narrative synthesis will be done alongside any meta-analysis and will be carried out using a framework which consists of four elements; 1- Developing a theory of how the intervention works, why and for whom. 2- Developing a preliminary synthesis of findings of included studies. 3- Exploring relationships within and between studies. 4- Assessing the robustness of the synthesis. |
Meta-analysis details what and how analysis and testing will be done. If no meta-analysis is to be conducted, please give a reason. | Although a meta-analysis is planned, this will only become apparent when we see what data is extracted and made available from the systematic review. Need to think about how heterogeneity will be explored. |
Grading evidence system used, if any, such as GRADE | GRADE will be used for evidence assessment. |
| |
Additional material summary tables, flowcharts, etc, to be included in the final paper | Flow chart of whole process Protocol Data extraction from and tables Forest plots of studies included in the final review |
Appendix C
Articles | Bias Arising from the Randomization Process | Bias Due to Deviations from Intended Interventions | Blinding of Participants and Personnel | Bias Due to Missing Outcome Data | Bias in Measurement of the Outcome | Bias in Selection of the Reported Result | Overall RoB |
---|---|---|---|---|---|---|---|
Marcus, 2013 [60] | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk |
Liu, 2017 [37] | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk |
Billings, 2020 [49] | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk |
Paruthi, 2016 [22] | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk | Low Risk |
Appendix D
Selection | Comparability | Outcome | Quality Score | Risk of Bias (0–3: High, 4–6: Moderate, 7–9: Low) | |||||
---|---|---|---|---|---|---|---|---|---|
Q1 | Q2 | Q3 | Q4 | Q5 | Q6 | Q7 | |||
Bergeron, 2021 [5] | * | * | * | * | * | * | * | Good Quality Study (7) | Low Risk |
Chervin, 2001 [3] | * | * | * | * | * | * | * | Moderate Quality Study (6) | Moderate Risk |
Brozek, 2020 [15] | ** | * | ** | ** | * | ** | ** | Good Quality Study (8) | Low Risk |
Mitchell, 2004 [24] | ** | * | ** | ** | ** | ** | ** | Good Quality Study (8) | Low Risk |
Wolraich, 2019 [56] | * | * | * | ** | * | * | * | Moderate Quality Study (6) | Moderate Risk |
Ye, 2010 [27] | ** | ** | ** | ** | ** | ** | ** | Good Quality Study (9) | Low Risk |
Appendix E
Selection | Comparability | Outcome | Quality Score | Risk of Bias (0–3: High, 4–6: Moderate, 7–9: Low) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
Article | Q1 | Q2 | Q3 | Q4 | Q5 | Q6 | Q7 | Q8 | ||
Clements, 2021 [4] | (C) Selected group of users | (C) No description of the derivation of the non-exposed cohort | * | * | No comparability | * | No | * | Poor Quality Study (4) | Moderate Risk |
Gozal, 2020 [7] | (C) Selected group of users | (C) No description of the derivation of the non-exposed cohort | * | * | No comparability | * | No | No | Poor Quality Study (3) | High Risk |
Alsharif, 2020 [9] | (C) Selected group of users | (A) derived from the same population | * | * | No comparability | * | No | * | Good Quality Study (7) | Low Risk |
Bhattacharjee, 2010 [10] | (C) Selected group of users | (C) No description of the derivation of the non-exposed cohort | * | * | No comparability | * | No | * | Poor Quality Study (4) | Moderate Risk |
Tunkel, 2008 [26] | (B) somewhat representative | (B) drawn from the same community | ** | ** | No comparability | ** | Yes | ** | Good Quality Study (8) | Low Risk |
Venekamp, 2015 [2] | (B) somewhat representative | (B) drawn from the same community | ** | ** | Two factors controlled | ** | Yes | ** | Good Quality Study (8) | Low Risk |
Zhang, 2017 [17] | (A) truly representative | (A) derived from the same population | ** | ** | One factor controlled | ** | Yes | * | Good Quality Study (7) | Low Risk |
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Authors | Country | Study Design | Year of Publication | Clinical Recommendations | Level of Evidence |
---|---|---|---|---|---|
Zhang et al. [17] | China | Prospective observational cohort study | 2017 | Clinicians should be vigilant about the potential impacts of OSA on bone development in affected patients. | III |
Domany et al. [18] | Ohio | Prospective study | 2019 | AT, the first-line treatment for OSA in children, has been shown to normalize PG in patients with OSA. This finding suggests that treating OSA can enhance the lungs’ ability to restore blood gas homeostasis following ventilatory disturbances. | III |
Biggs et al. [19] | Australia | Four-year longitudinal study | 2014 | Treating SDB in children may improve neurocognitive functions, particularly performance IQ tasks like spatial visualization, visual-motor coordination, and abstract reasoning. | III |
Lushington et al. [20] | Australia | Prospective study | 2021 | Educate parents on the potential for significant improvements in their child’s sleep quality and overall quality of life following AT, even if noticeable behavioral changes are less evident. | III |
Yu et al. [21] | China | RCTs | 2015 | For moderate to severe OSA, surgery is the primary treatment. In cases of mild OSA, LTRAs are recommended, with surgery as a consideration if drug therapy proves ineffective. | I |
Paruthi et al. [22] | USA | RCTs | 2016 | The study identified a high prevalence of sleepiness in children with OSA, even in the absence of prolonged oxygen desaturation. | I |
Giordani et al. [23] | USA | Cohort study | 2012 | Conduct routine PSG before and after AT to assess improvements in the OAI and identify any residual SDB postoperatively, particularly in children with confirmed OSA. | III |
Mitchell et al. [24] | Mexico | Prospective study | 2004 | Schedule post-operative PSG approximately 5 to 6 months after AT to evaluate changes in the RDI and assess the efficacy of the surgery. | III |
Tran et al. [25] | USA | Prospective study | 2005 | OSA-18 questionnaire to assess the severity of SDB and its impact on the quality of life in children with OSA. | III |
Tunkel et al. [26] | USA | Prospective study | 2008 | Utilize PSG for precise diagnosis and classification of OSA prior to surgical intervention. | III |
Ye et al. [27] | China | Cross-sectional study | 2010 | Consider the pre-operative severity of OSA and obesity when selecting patients for AT, as these factors signifi-cantly influence post-operative outcomes. | III |
Arima et al. [28] | Japan | Retrospective study | 2019 | Following AT, monitor BMI scores regularly as a significant increase has been observed post-surgery. | III |
Koren et al. [29] | USA | Prospective study | 2016 | Post-operative PSG should be routinely performed in children following AT, as residual OSA is common, espe-cially in those with obesity. | III |
Tagaya et al. [30] | Japan | Prospective study | 2012 | Screen and manage allergic rhinitis and other allergic diseases both preoperatively and postoperatively, as these conditions are more prevalent in children with persistent OSA symptoms. | III |
Nath et al. [31] | USA | Retrospective study | 2013 | Be aware that predictors of persistent or residual OSA after AT in young children include older age, higher BMI, the presence of asthma, and more severe pre-operative OSA as measured by the AHI. | III |
Bhushan et al. [32] | USA | Retrospective study | 2014 | Assess cognitive and visual-motor function using the VMI test before surgery to evaluate visual-motor integration abilities and gain insight into potential neurocognitive deficits associated with OSA. | III |
Mitchell [33] | USA | Prospective cohort study | 2007 | AT significantly improves respiratory parameters in children with OSA, as measured by PSG. | III |
Al-Zaabi et al. [34] | Oman | Observational cohort study | 2019 | Conduct follow-up assessments within 3 months post-AT to capture early neurocognitive and behavioral changes. This timeframe is generally sufficient for evaluating improvements and guiding further interventions. | III |
Li et al. [35] | Taiwan | Prospective cohort study | 2006 | For children diagnosed with SDB, particularly those with enlarged tonsils and adenoids, AT is recommended. | III |
Nieminen et al. [36] | Finland | Prospective cohort study | 2002 | Collaborate among pediatricians, ENT specialists, and endocrinologists to effectively manage OSA and associated growth issues. | III |
Liu et al. [37] | Taiwan | Retrospective cohort study | 2016 | Use nocturnal oximetry as a cost-effective alternative for post-surgery follow-up, especially to detect residual mild OSA. | III |
Lee CH et al. [38] | Taiwan | Retrospective study | 2018 | Monitor post-operative BP regularly, as significant improvements in BP may be observed following AT. | III |
Hsu et al. [39] | Taiwan | Prospective cohort study | 2018 | Collaborate with pediatricians, cardiologists, and sleep specialists to provide comprehensive care for children with OSA and hypertension. | III |
De Magalhães et al. [40] | Brazil | Prospective comparative study | 2019 | Regularly monitor blood oxygen saturation in post-operative patients. Levels below 90% are considered hypoxemic and should be addressed immediately. | III |
Song et al. [41] | Korea | Prospective cohort study | 2019 | Apply AT in children with severe OSA and monitor for age-related physiological changes that may influence outcomes. | III |
Kuo et al. [42] | Taiwan | Prospective cohort study | 2015 | Ensure a thorough assessment of clinical history and PSG results before considering AT or other treatments. | III |
Suri et al. [43] | India | Prospective interventional study | 2015 | Screen children early for OSA symptoms, particularly those with adenotonsillar hypertrophy and craniofacial anomalies. Consider performing AT at a younger age (preferably before 8 years) for better outcomes. | III |
Lee SY et al. [44] | USA | Retrospective cohort study | 2015 | Conduct PSG immediately after AT and at follow-up intervals (e.g., 6 months, 12 months) to evaluate residual SDB and mouth breathing. | III |
Bhattacharjee et al. [45] | USA | Retrospective cohort study | 2016 | Investigate additional biomarkers and methods to predict residual OSA and enhance treatment outcomes. | III |
Kaditis et al. [46] | Greece | Prospective cohort study | 2011 | Monitor BNP levels as an indicator of cardiac strain and ventricular load. A reduction in BNP levels following AT suggests decreased cardiac strain. | III |
Kobayashi et al. [47] | Japan | Prospective observational study | 2014 | Use the A/N ratio to determine the type of surgery required. AT should be considered for patients with an A/N ratio ≥ 0.55, while tonsillectomy may be appropriate for those with an A/N ratio < 0.55. | III |
Villa et al. [48] | Italy | Prospective cohort study | 2013 | AT is recommended for younger children with severe OSA, particularly those with dental malocclusions and a narrow palate. | III |
Billings et al. [49] | USA | Retrospective study | 2020 | Admit patients with severe OSA (AHI >20 events/hour, SpO2 nadir <80%) to the PICU for close post-operative monitoring. | III |
Hamada et al. [50] | Japan | Retrospective study | 2015 | Perform AT as the primary treatment for OSA in infants and toddlers, considering it safe and effective when performed without significant comorbidities. | III |
Chung et al. [51] | USA | Prospective cohort study | 2015 | AT leads to behavioral improvements in children with sleep-disordered breathing, regardless of their intellectual ability. | III |
Wei et al. [52] | USA | Prospective study | 2007 | AT significantly improves both sleep and behavior in children diagnosed with SDB. | III |
Outcome Measure | 0–5 Years | 6–7 Years | 8–10 Years | >10 Years |
---|---|---|---|---|
AHI reduction (%) | 86% | 82% | 74% | 62% |
Mean AHI pre-AT (events/hour) | 12.5 ± 3.2 | 14.2 ± 4.0 | 16.1 ± 3.9 | 18.5 ± 4.5 |
Mean AHI post-AT (events/hour) | 1.8 ± 0.9 | 2.5 ± 1.1 | 4.2 ± 1.5 | 7.0 ± 2.2 |
ODI improvement (%) | 88% | 84% | 78% | 70% |
Mean SpO2 Nadir pre-AT (%) | 86.7% | 87.5% | 89.2% | 90.1% |
Mean SpO2 Nadir post-AT (%) | 95.1% | 94.6% | 93.5% | 92.5% |
Sleep efficiency improvement | Significant | Moderate | Moderate | Low |
Neurocognitive/behavioral improvement | High | High | Moderate | Low |
Post-operative Bleeding Rate (%) | 2.1% | 3.2% | 4.7% | 6.5% |
Extended Post-operative Pain (%) | Low | Low | Moderate | High |
Transient Airway Obstruction (%) | 5.3% | 4.1% | 2.8% | 1.9% |
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Halawani, M.; Alsharif, A.; Alanazi, O.I.; Awad, B.; Alsharif, A.; Alahmadi, H.; Alqarni, R.; Alhindi, R.M.; Alanazi, A.H.; Alshamrani, A.H. Efficacy and Safety of Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Across Various Age Groups: A Systematic Review. Pediatr. Rep. 2025, 17, 71. https://doi.org/10.3390/pediatric17040071
Halawani M, Alsharif A, Alanazi OI, Awad B, Alsharif A, Alahmadi H, Alqarni R, Alhindi RM, Alanazi AH, Alshamrani AH. Efficacy and Safety of Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Across Various Age Groups: A Systematic Review. Pediatric Reports. 2025; 17(4):71. https://doi.org/10.3390/pediatric17040071
Chicago/Turabian StyleHalawani, Mohammed, Arwa Alsharif, Omar Ibrahim Alanazi, Baraa Awad, Abdulaziz Alsharif, Hawazen Alahmadi, Rayan Alqarni, Rahaf Mohammed Alhindi, Abdulmohsen H. Alanazi, and Abdulmajeed Hassan Alshamrani. 2025. "Efficacy and Safety of Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Across Various Age Groups: A Systematic Review" Pediatric Reports 17, no. 4: 71. https://doi.org/10.3390/pediatric17040071
APA StyleHalawani, M., Alsharif, A., Alanazi, O. I., Awad, B., Alsharif, A., Alahmadi, H., Alqarni, R., Alhindi, R. M., Alanazi, A. H., & Alshamrani, A. H. (2025). Efficacy and Safety of Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Across Various Age Groups: A Systematic Review. Pediatric Reports, 17(4), 71. https://doi.org/10.3390/pediatric17040071